Jean-BaptisteLe PichonMD, PhD, FAAP

PubMed

• 100 citations
  Clinical Presentation of a Complex Neurodevelopmental Disorder Caused by Mutations in ADNP
  Anke Van Dijck, Anneke T. Vulto-van Silfhout, Elisa Cappuyns, Ilse M. van der Werf, Grazia M.S. Mancini
  Biological Psychiatry. 2019-02-15
• 11 citations
  The efficacy and tolerability of auto-stimulation-VNS in children with Lennox-Gastaut syndrome.
  Sherouk A Abdelmoity, Ayman A. Abdelmoity, Sean M. Riordan, Christian Kaufman, Jean-Baptiste Le Pichon
  Seizure. 2021-03-01
• 15 citations
  Initiating the ketogenic diet in infants with treatment refractory epilepsy while maintaining a breast milk diet.
  J.B. Le Pichon, Lindsey M Thompson, Megan Gustafson, Ahmed Abdelmoity
  Seizure. 2019-07-01

Journal Articles

• Brown-Vialetto-Van Laere Syndrome as a Mimic of Neuroimmune Disorders: 3 Cases From the Clinic and Review of the Literature  
  Allison, T., Roncero, I., Forsyth, R., Coffman, K., & Pichon, J. B. L., Journal of Child Neurology, 1/1/2017
• A Hypothesis for Using Pathway Genetic Load Analysis for Understanding Complex Outcomes in Bilirubin Encephalopathy  
  Sean M. Riordan, Douglas C. Bittel, Jean-Baptiste Le Pichon, Silvia Gazzin, Claudio Tiribelli, Jon F. Watchko, Richard P.Wennberg, and Steven M. Shapiro, Frontiers in Neuroscience, 1/1/2016
• Biallelic Mutations in TBCD, Encoding the Tubulin Folding Cofactor D, Perturb Microtubule Dynamics and Cause Early-Onset Encephalopathy  
  Flex E, Niceta M, Cecchetti S, Thiffault I, Au MG, Capuano A, Piermarini E, Ivanova AA, Francis JW, Chillemi G, Chandramouli B, Carpentieri G, Haaxma CA, Ciolfi A, Piz..., American Journal of Human Genetics, 1/1/2016
• Hyperactivity in the Gunn rat model of neonatal jaundice: age-related attenuation and emergence of gait deficits  
  Stanford, J.A., Shuler, Jeffrey M., Fowler, S.C., Stanford, K.G., Ma, D., Bittel, D.C., Le Pichon, J.B., Shapiro, S.M., Pediatric Research, 1/14/2015
• The Future of Next-Generation Sequencing in Neurology  
  LePichon, Jean-Baptiste, MD, PhD, Saunders, Carol J., PhD, Soden, Sarah E., MD, JAMA Neurology, 1/1/2015
• Loss of Function Variants in Human PNPLA8 Encoding Calcium-Independent Phospholipase A2 ? Recapitulate the Mitochondriopathy of the Homologous Null Mouse  
  Saunders CJ, Moon SH, Liu X, Thiffault I, Coffman K, LePichon JB, Taboada E, Smith LD, Farrow EG, Miller N, Gibson M, Patterson M, Kingsmore SF, Gross RW, Hum Mutat, 1/1/2014
• A Refresher on Tourette Syndrome  
  Batterson, J., Sullivant, S,. Le Pichon, J.B., Kleinsorge, C., Price, S., Andrews, S., Missouri Medicine, 1/1/2014
• Effectiveness of exome and genome sequencing guided by acuity of illness for diagnosis of neurodevelopmental disorders  
  Soden, Sarah E., Carol J. Saunders, Laurel K. Willig, Emily G. Farrow, Laurie D. Smith, Josh E. Petrikin, Jean-Baptiste LePichon, Neil A. Miller, Isabelle Thiffault, D..., Science translational medicine, 1/1/2014
• Genome-wide gene expression in a patient with 15q133 homozygous microdeletion syndrome  
  Le Pichon, J.B., Yu, S., Kibiryeva, N., Graf, W., & Bittel, D., European Journal of Human Genetics, 1/1/2013
• 15q112 proximal imbalances associated with a diverse array of neuropsychiatric disorders and mild dysmorphic features  
  Abdelmoity, A., Le Pichon, J.B., Nyp, S., Soden, S., Daniel, C., & Yu, S., Journal of Developmental & Behavioral Pediatrics, 1/1/2012
• Practice parameter: evaluation of the child with microcephaly (an evidence-based review) Letter to the Editor  
  Graf, W., Le Pichon, J.B., Bittel, D., Abdelmoity, A., & Yu, S., American Academy of Neurology, 1/1/2010
• A 15q133 homozygous microdeletion associated with a severe neurodevelopmental disorder suggests putative functions of the trpm1, chrna7, and other homozygously deleted...  
  Le Pichon, J.B., Bittel, D., Graf, W., & Yu, S., American Journal of Medical Genetics, 1/1/2010
• Ethosuximide, valproic acid, and lamotrigine in childhood absence epilepsy  
  Glauser, T., Cnaan, A., Hirtz, D., Dlugos, D., Masur, D., Clark, P., Capparelli, E., Clark, P., Adamson, P. & for the Childhood Absence Epilepsy Study Group; EEG/Clini..., New England Journal of Medicine, 1/1/2010
• Join now to see all

Books/Book Chapters

• Neonatology: Clinical Practice and Procedures 
  Chapter: Neonatal Hypotonia. 
  Page 211 - 223Le Pichon JB, Shapiro S.M.Editors: Stevenson D, Cohen R, Sunshine P.McGraw HillEdition 1st,2015
• Toward A Science of Consciousness: "Tucson III" 
  Chapter: Experimental predictions based on the statistical and temporal aspects of a hypothetical neural mechanism for subjectivity. 
  Helekar, S., & Le Pichon, J.B.University of Arizona, Tucson, AZ1998

Abstracts/Posters

• Escaping X-inactivation: A New Perspective on KIAA2022-Related Disorders: Allosome Imprinting & Sexual Phenotypic Dimorphism.
  Jean-Baptiste Le Pichon, Carol Saunders, Emily Farrow, Sarah Soden, Sumit Parikh, Isabelle Thiffault, Child Neurology Society, 45th Annual Meeting, Vancouver, British Columbia, Canada, 1/1/2016
• Poster 76. Brown-Vialetto-Van Laere Syndrome Mistaken for Neuroimmune Disorders: Three Cases from the Clinic and Review of the Literature.
  Allison, T.J., Forsyth, R., Coffman, K.A., Le Pichon, JB, Child Neurology Society, 44th Annual Meeting, Washington, DC, 1/1/2015
• What are the Molecular Mechanisms that Govern Region Specific Vulnerability to Bilirubin in the Central Nervous System?
  Le Pichon, J.B., Bittel, D., Shapiro, S., Pediatric Academic Societies and Asian Society for Pediatric Research Joint Meeting, Vancouver, British Columbia, Canada, 1/1/2014
• Utility of exome sequencing in the evaluation of neurodevelopmental disorders.
  Le Pichon, J.B., Abdelmoity, A., Soden, S., Smith, L., Modrcin, A., Saunders, C., Farrow, E., Dinwiddie, D., Miller, N., Atherton, A., Kingsmore, S., Child Neurology Society, 42nd Annual Meeting, 1/1/2013
• What is the clinical utility of chromosomal microarray testing in general child neurology practice?
  Le Pichon, J.B., Luniova, A., Yuen, J., Abdelmoity, A., Allaboun, K., Sherman, A., Haney, C., Yu, S., Graf, W., Child Neurology Society, 41st Annual Meeting, 1/1/2012
• Genomic testing by 244K oligonucleotide microarray CGH in primary microcephaly: predictive value of additional clinical findings.
  Abdelmoity, A., Yu, S., Le Pichon, J.B., Allaboun, K., Womelduff, G., Sherman, A., Bittel, D., Graf, W., Annals of Neurology, 1/1/2009
• The "phenotype first" to "genotype first" paradigm shift: rethinking genomic discovery using microarray (aCGH) and the neuroethics of incidental findings.
  Graf, W., Le Pichon, J.B., Abdelmoity, A., Sherman, A., Bittel, D., Yu, S., Annals of Neurology, 1/1/2009
• Predictive clinical findings associated with genomic disorders in unexplained primary intellectual disability.
  Le Pichon, J.B., Allaboun, K., Graf, W., Abdelmoity, A., Womelduff, G., Sherman, A., Bittel, D., Yu, S., Annals of Neurology, 1/1/2009
• Ketogenic diet efficacy in children with pharmacologically intractable epilepsy of different types.
  Abdelmoity, A., Driscol, V., Thomson, L., Le Pichon, J.B., Epilepsia; American Epilepsy Society, 63rd Annual Meeting, 1/1/2009
• Parents' perspective on quality of life improvement in patients with intractable epilepsy receiving a ketogenic diet.
  Driscol, V., Le Pichon, J.B., Thomson, L., Vaughn, L., Womelduff, G., Abdelmoity, A., Epilepsia; American Epilepsy Society, 63rd Annual Meeting, 1/1/2009
• Outcome following VNS placement in children in a single large tertiary care institution.
  Le Pichon, J.B., Baker, M., Abid, F., Chapman, K., & Wilfong, A., Epilepsia, 1/1/2005
• Identification of new residues contributing to the binding site of the neuronal nicotinic alpha7 receptor.
  Le Pichon, J.B., & Patrick, J., Society for Neuroscience, 27th Annual Meeting, New Orleans, LA, 1/1/1997
• Alpha7 receptor function is rescued from cyclosporin block by coexpression with muscle delta subunit.
  Colquhoun, L., Le Pichon, J.B., Vollrath, M., & Patrick, J., Society for Neuroscience, 24th Annual Meeting, Miami Beach, FL, 1/1/1994
• Join now to see all

Lectures

• Exomes, Genomes, GWAS and Still No Answers-Gee Whiz, Where Do We Go Next? 
  University of Kansas Medical Center, Kansas City, KS - 1/13/2017
• Point and Counterpoint: Treating Neonatal Subclinical Seizures or Not. 
  Kansas City, MO - 1/8/2016
• Standard Protocol for Initiating AED Therapy in Newborns 
  Inn on Biltmore Estates, Asheville, NC - 1/28/2015
• Enterovirus D68 and Acute Flaccid Myelitis, a Onetime Epidemic or a Sign of Things to Come? 
  Inn on Biltmore Estates, Asheville, NC - 1/27/2015
• The Acute Flaccid Myelitis Epidemic of 2014: Isolated Incident or a Sign of More to Come? 
  University of Kansas Medical Center, Kansas City, KS - 1/13/2015
• EV D68 Associated Acute Flaccid Myelitis 
  Cheshire Inn, St. Louis, MO - 1/10/2015
• Background: Enteroviruses and Acute Flaccid Myelitis Historical Review and Insights into the Neuropathology. 
  Washington, DC - 1/8/2015
• Progress Towards a Bilirubin Encephalopathy Susceptibility Gene Panel. 
  Trieste, Italy - 1/3/2015
• Epilepsy Classification and Management 
  University of Kansas Medical Center, Kansas City, KS - 1/21/2014
• A Medical Home for Patients with Tourette Syndrome 
  Children's Mercy Hospitals & Clinics, Kansas City, MO - 1/1/2014
• What are the Molecular Mechanisms that Govern Selective Vulnerability in the CNS? An Old Problem Re-examined in the Light of New Technologies 
  Trieste, Italy - 1/29/2013
• History, Diagnosis and Treatment of Tic Disorders 
  Kansas City, MO - 1/27/2013
• Next-Generation Sequencing & Comparative Genomic Hybridization, the Good, the Bad, and the Ugly. The Children's Mercy Experience 
  University of Kansas Medical Center, Kansas City, KS - 1/3/2013
• Movement Disorders in Children 
  Research Medical Center Brookside Campus, Kansas City, MO - 1/26/2012
• Tourette Syndrome 
  Derby High School, Derby, KS - 1/23/2012
• Tics and Tourette Syndrome: to Treat or not to Treat 
  Hapuna Beach Prince Hotel, HI - 1/18/2012
• Concussions: an Old Problem, a New Approach 
  Hapuna Beach Prince Hotel, HI - 1/18/2012
• Seizures and Epilepsy: What to do While I Wait for the Neurology Referral? 
  Hapuna Beach Prince Hotel, HI - 1/16/2012
• Pediatric Headaches: a Rational Approach to a Common Problem 
  Hapuna Beach Prince Hotel, HI - 1/16/2012
• Tics or Tourette's 
  Children's Mercy Hospital, Kansas City, MO - 1/14/2012
• Neurogenetic from Phenotype to Genotype and Back 
  University of Kansas Medical Center, Kansas City, KS - 1/3/2012
• Headaches for Allergist/Immunologist 
  Children's Mercy Hospitals & Clinics - 1/27/2011
• Seizures and Breath holding Spells 
  Riverside Elementary, Emporia, KS - 1/24/2011
• Lunch and Learn 
  Emporia, KS - 1/24/2011
• Tics, Tremors and Tourette Syndrome 
  Research Hospital, Kansas City, MO - 1/28/2010
• Join now to see all

Other

• Inside Pediatrics Children's Mercy Kansas City Season 2 
  Le Pichon, J.B., KMBC-TV
  Kansas City, MO - 1/1/2015
• Cases of Acute Flaccid Myelitis in Children Suspected in Multiple States, Prompting Comparisons to Polio 
  Dan Hurley, Article-In-Brief, comment by Dr. Le Pichon, Neurology Today
  1/6/2014
• Inside Pediatrics Children’s Mercy Kansas City Season 1 
  Le Pichon, J.B., KMBC-TV
  Kansas City, MO - 1/1/2014
• Autoimmune Movement Disorders 
  Le Pichon, J.B., KCTV 5 Kansas City CBS, MO
  1/22/2012
• Concussions 
  Le Pichon, J.B., Sports Radio 810WHB
  1/2/2011
• Join now to see all